Author:
Suter Bernhard,Treadwell-Deering Diane,Zoghbi Huda Y.,Glaze Daniel G.,Neul Jeffrey L.
Publisher
Springer Science and Business Media LLC
Subject
Developmental and Educational Psychology
Reference27 articles.
1. Allen, R. C., Zoghbi, H. Y., Moseley, A. B., Rosenblatt, H. M., & Belmont, J. W. (1992). Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation. American Journal of Human Genetics, 51(6), 1229–1239.
2. Amir, R. E., Van den Veyver, I. B., Wan, M., Tran, C. Q., Francke, U., & Zoghbi, H. Y. (1999). Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. Nature Genetics, 23(2), 185–188. doi: 10.1038/13810 .
3. Bebbington, A., Anderson, A., Ravine, D., Fyfe, S., Pineda, M., de Klerk, N., et al. (2008). Investigating genotype-phenotype relationships in Rett syndrome using an international data set. Neurology, 70(11), 868–875. doi: 10.1212/01.wnl.0000304752.50773.ec .
4. Bebbington, A., Percy, A., Christodoulou, J., Ravine, D., Ho, G., Jacoby, P., et al. (2010). Updating the profile of C-terminal MECP2 deletions in Rett syndrome. Journal of Medical Genetics, 47(4), 242–248.
5. Beyer, K. S., Blasi, F., Bacchelli, E., Klauck, S. M., Maestrini, E., & Poustka, A. (2002). Mutation analysis of the coding sequence of the MECP2 gene in infantile autism. Human Genetics, 111(4–5), 305–309. doi: 10.1007/s00439-002-0786-3 .
Cited by
33 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献